INACTIVATION OF PANCREATIC AND GASTRIC LIPASES BY THL AND C-12-0-TNB - A KINETIC-STUDY WITH EMULSIFIED TRIBUTYRIN

被引:69
作者
GARGOURI, Y
CHAHINIAN, H
MOREAU, H
RANSAC, S
VERGER, R
机构
[1] CNRS,CTR BIOCHIM & BIOL MOLEC,BP 71,F-13402 MARSEILLE 9,FRANCE
[2] ECOLE NATL INGENIEURS SFAX,BIOCHIM LAB,SFAX,TUNISIA
关键词
PANCREATIC LIPASE; GASTRIC LIPASE; ENZYME INACTIVATION;
D O I
10.1016/0005-2760(91)90136-6
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
THL is a potent inhibitor of pancreatic (PPL) and gastric (HGL, RGL) lipases. Inactivation occurs preferentially at the oil/water interface (method B, C). In the aqueous phase (method A), the inhibition of HGL was accelerated by the presence of bile salts. C12:0-TNB, a disulfide reagent, specifically inactivates gastric lipases and had no effect on the pancreatic lipase (in the presence of bile salts) whatever the method used. The capacity of THL and C12:0-TNB to inactivate lipases using Methods B and C was found to depend directly upon the interfacial area of the system used. Consequently, inactivation can be reduced or prevented by further addition of a water-insoluble substrate which reduces the surface density of inactivator molecules. With a heterogeneous system of this kind, typical of lipolysis, the use of a classical Michaelis-Menten model is irrelevant and hence the traditional kinetic parameters (K(m), K(I), V(max)) are only apparent values.
引用
收藏
页码:322 / 328
页数:7
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